Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs57095329
MIR3142HG
0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs2606345
CYP1A1
0.732 0.360 15 74724835 intron variant C/A snv 0.46 16
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs3789243
ABCB1
0.776 0.120 7 87591570 intron variant A/G snv 0.50 14
rs4906902
GABRB3
0.724 0.200 15 26774621 intron variant A/G snv 0.15 14
rs694539
NNMT
0.776 0.200 11 114262697 intron variant C/T snv 0.21 10
rs4523957
SMG6 ; SRR
0.790 0.120 17 2305605 intron variant G/T snv 0.54 9
rs3755724
TIMP4 ; SYN2
0.790 0.360 3 12159406 intron variant C/T snv 0.31 8
rs3761847
TRAF1
0.827 0.200 9 120927961 intron variant G/A snv 0.52 8
rs10868235
NTRK2
0.925 0.040 9 84878840 intron variant C/T snv 0.40 6
rs2920502
PPARG
0.851 0.160 3 12287696 intron variant G/C snv 0.27 6
rs7127507
BDNF-AS ; BDNF
0.827 0.080 11 27693337 intron variant T/C snv 0.34 6
rs12912233
RORA
0.851 0.120 15 60974897 intron variant C/T snv 0.38 5
rs59007384
TOMM40
0.851 0.080 19 44893408 intron variant G/A;T snv 4
rs3903529
RORB
0.882 0.120 9 74649312 intron variant T/A snv 0.23 3
rs992670
C5
0.882 0.120 9 121019492 intron variant G/A snv 0.52 3
rs10157763
AKT3
1.000 0.040 1 243831739 intron variant T/A;C snv 2
rs1178326
HDAC9
1.000 0.040 7 18195234 intron variant T/C snv 3.9E-02 2
rs12059546
CHRM3
0.925 0.040 1 239806797 intron variant A/G snv 0.30 2
rs12668095
LOC105375268
1.000 0.040 7 47036178 intron variant G/A;C snv 2
rs13287547
C9orf92
1.000 0.040 9 16286892 intron variant A/G snv 0.32 2
rs141860749
SYT2
1.000 0.040 1 202668176 intron variant C/A snv 2.7E-04 2